Aurobindo Pharma Limited, Unit XI
FDA inspection history in Pydibhimavaram, India, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Pydibhimavaram, India.
Cited most
Across all Aurobindo Pharma Limited, Unit XI observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Aurobindo Pharma Limited, Unit XI file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pydibhimavaram, India
One Form 483 · 2022 · 3 observations
Latest: Form 483, Aug 2, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-08-02 | 483 Form 483 | Pydibhimavaram, India | 3 | $99 |
Investigators on these documents
FEI number 3004611 · most recent document Aug 2, 2022
About Aurobindo Pharma Limited, Unit XI
How many FDA Form 483s has Aurobindo Pharma Limited, Unit XI received?
FDA Intel has 1 Form 483 on file for Aurobindo Pharma Limited, Unit XI; the most recent is dated Aug 2, 2022.
When was Aurobindo Pharma Limited, Unit XI last inspected by FDA?
The most recent FDA inspection document on file for Aurobindo Pharma Limited, Unit XI is a Form 483 dated Aug 2, 2022, for the site in Pydibhimavaram, India.
What did FDA cite at Aurobindo Pharma Limited, Unit XI?
The regulations cited most in the observations on file for Aurobindo Pharma Limited, Unit XI are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.